U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C8H8O5
Molecular Weight 184.1461
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3,4-DIHYDROXYMANDELIC ACID

SMILES

OC(C(O)=O)C1=CC=C(O)C(O)=C1

InChI

InChIKey=RGHMISIYKIHAJW-UHFFFAOYSA-N
InChI=1S/C8H8O5/c9-5-2-1-4(3-6(5)10)7(11)8(12)13/h1-3,7,9-11H,(H,12,13)

HIDE SMILES / InChI

Molecular Formula C8H8O5
Molecular Weight 184.1461
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Thu Jul 06 23:29:19 UTC 2023
Edited
by admin
on Thu Jul 06 23:29:19 UTC 2023
Record UNII
WDP6VCX5T6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3,4-DIHYDROXYMANDELIC ACID
Systematic Name English
(±)-3,4-DIHYDROXYMANDELIC ACID
Systematic Name English
.ALPHA.,3,4-TRIHYDROXYBENZENEACETIC ACID
Systematic Name English
Benzeneacetic acid, α,3,4-trihydroxy-
Systematic Name English
α-Hydroxy-3,4-dihydroxyphenylacetic acid
Systematic Name English
DL-3,4-Dihydroxymandelic acid
Systematic Name English
DOMA
Common Name English
MANDELIC ACID, 3,4-DIHYDROXY-
Systematic Name English
Code System Code Type Description
PUBCHEM
85782
Created by admin on Thu Jul 06 23:29:19 UTC 2023 , Edited by admin on Thu Jul 06 23:29:19 UTC 2023
PRIMARY
CAS
775-01-9
Created by admin on Thu Jul 06 23:29:19 UTC 2023 , Edited by admin on Thu Jul 06 23:29:19 UTC 2023
PRIMARY
WIKIPEDIA
3,4-Dihydroxymandelic acid
Created by admin on Thu Jul 06 23:29:19 UTC 2023 , Edited by admin on Thu Jul 06 23:29:19 UTC 2023
PRIMARY
EPA CompTox
DTXSID30862411
Created by admin on Thu Jul 06 23:29:19 UTC 2023 , Edited by admin on Thu Jul 06 23:29:19 UTC 2023
PRIMARY
FDA UNII
WDP6VCX5T6
Created by admin on Thu Jul 06 23:29:19 UTC 2023 , Edited by admin on Thu Jul 06 23:29:19 UTC 2023
PRIMARY
CHEBI
27637
Created by admin on Thu Jul 06 23:29:19 UTC 2023 , Edited by admin on Thu Jul 06 23:29:19 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE